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CX3CL1 anticorps

Cet anticorps Lapin Monoclonal détecte spécifiquement CX3CL1 dans WB et IF. Il présente une réactivité envers Humain.
N° du produit ABIN1683181

Aperçu rapide pour CX3CL1 anticorps (ABIN1683181)

Antigène

Voir toutes CX3CL1 Anticorps
CX3CL1 (Chemokine (C-X3-C Motif) Ligand 1 (CX3CL1))

Reactivité

  • 79
  • 39
  • 31
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 78
  • 11
  • 3
  • 2
  • 1
Lapin

Clonalité

  • 82
  • 13
Monoclonal

Conjugué

  • 52
  • 11
  • 7
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp CX3CL1 est non-conjugé

Application

  • 78
  • 30
  • 26
  • 23
  • 15
  • 13
  • 13
  • 12
  • 7
  • 6
  • 6
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  •  Réactivité croisée

    Humain, Souris, Rat

    Attributs du produit

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogène

    A synthesized peptide derived from human PMP70/ABCD3

    Isotype

    IgG
  • Indications d'application

    WB,1:500 - 1:2000,IF,1:50 - 1:200

    Restrictions

    For Research Use only
  • Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène

    CX3CL1 (Chemokine (C-X3-C Motif) Ligand 1 (CX3CL1))

    Autre désignation

    ABCD3

    Sujet

    The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ALD subfamily, which is involved in peroxisomal import of fatty acids and/or fatty acyl-CoAs in the organelle. All known peroxisomal ABC transporters are half transporters which require a partner half transporter molecule to form a functional homodimeric or heterodimeric transporter. This peroxisomal membrane protein likely plays an important role in peroxisome biogenesis. Mutations have been associated with some forms of Zellweger syndrome, a heterogeneous group of peroxisome assembly disorders. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008],ABC43, CBAS5, PMP70, PXMP1, ZWS2,Cancer,Endocrine & Metabolism,Lipid Metabolism,Neurodegenerative Diseases,Neurodegenerative Diseases_Amyloid Plaque and Neurofibrillary Tangle Formation in Alzheimers Disease,Neuroscience,Signal Transduction,ABCD3

    Poids moléculaire

    70 kDa

    ID gène

    5825

    UniProt

    P28288

    Pathways

    Synaptic Membrane
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